A flexible and accurate genotype imputation method for the next generation of genome-wide association studies (Q21129496)

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scientific article published in June 2009

• A Flexible and Accurate Genotype Imputation Method for the Next Generation of Genome-Wide Association Studies

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English	A flexible and accurate genotype imputation method for the next generation of genome-wide association studies	scientific article published in June 2009	A Flexible and Accurate Genotype Imputation Method for the Next Generation of Genome-Wide Association Studies

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instance of

scholarly article

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title

A flexible and accurate genotype imputation method for the next generation of genome-wide association studies (English)

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main subject

genome-wide association study

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imputation

1 reference

based on heuristic

inferred from title

author

Peter Donnelly

series ordinal

2

object named as

Peter Donnelly

author given names

Peter

author last names

Donnelly

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stated in

PubMed

PubMed publication ID

19543373

retrieved

16 August 2022

Jonathan Marchini

series ordinal

3

object named as

Jonathan Marchini

author given names

Jonathan

author last names

Marchini

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stated in

PubMed

PubMed publication ID

19543373

retrieved

16 August 2022

author name string

Bryan N Howie

series ordinal

1

author given names

Bryan N

author last names

Howie

1 reference

stated in

PubMed

PubMed publication ID

19543373

retrieved

16 August 2022

language of work or name

English

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publication date

June 2009

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published in

PLOS Genetics

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volume

5

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issue

6

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page(s)

e1000529

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copyright license

Creative Commons Attribution 4.0 International

start time

19 June 2009

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April 2022 Public Data File from Crossref

copyright status

copyrighted

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cites work

Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes

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A unified approach to genotype imputation and haplotype-phase inference for large data sets of trios and unrelated individuals

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19 March 2017

Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease

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19 March 2017

A second generation human haplotype map of over 3.1 million SNPs

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19 March 2017

Rapid and accurate haplotype phasing and missing-data inference for whole-genome association studies by use of localized haplotype clustering

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PLINK: a tool set for whole-genome association and population-based linkage analyses

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19 March 2017

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

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19 March 2017

Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis

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19 March 2017

A fast and flexible statistical model for large-scale population genotype data: applications to inferring missing genotypes and haplotypic phase

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PubMed Central

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19 March 2017

Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes

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PubMed Central

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7 April 2017

A new multipoint method for genome-wide association studies by imputation of genotypes

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PubMed Central

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7 April 2017

A fine-scale map of recombination rates and hotspots across the human genome

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7 April 2017

Genotype-imputation accuracy across worldwide human populations

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PubMed Central

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12 September 2017

Detection of sharing by descent, long-range phasing and haplotype imputation

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12 September 2017

Imputation of missing genotypes: an empirical evaluation of IMPUTE.

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12 September 2017

Practical issues in imputation-based association mapping

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12 September 2017

Simple and efficient analysis of disease association with missing genotype data

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12 September 2017

Imputation-based analysis of association studies: candidate regions and quantitative traits

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A comparison of phasing algorithms for trios and unrelated individuals

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PubMed Central

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12 September 2017

Modeling linkage disequilibrium and identifying recombination hotspots using single-nucleotide polymorphism data

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PubMed Central

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12 September 2017

Genome-wide association study identifies a second prostate cancer susceptibility variant at 8q24.

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PubMed Central

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retrieved

29 November 2018

Testing untyped alleles (TUNA)-applications to genome-wide association studies.

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2689936

retrieved

29 November 2018

Identifiers

DOI

10.1371/JOURNAL.PGEN.1000529

1 reference

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

190914

OpenCitations bibliographic resource ID

190914

1 reference

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

190914

PMC publication ID

2689936

1 reference

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

190914

PubMed publication ID

19543373

1 reference

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

190914

ResearchGate publication ID

26308064

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